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RSPH3
RSPH3 (NM 031924) Human Recombinant Protein – TP761392
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Next Generation Massively Parallel Sequencing of Targeted
Transposon Activation Mutagenesis As a Screening Tool for Identifying
Cldn19 Clic2 Clmp Cln3
Ciliary Dyneins and Dynein Related Ciliopathies
Notch/Her12 Signalling Modulates, Motile/Immotile Cilia Ratio
The Conserved Ancestral Signaling Pathway from Cilium to Nucleus Peter Satir1,2,* and Birgit H
Novel Gene Discovery in Primary Ciliary Dyskinesia
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
Relationship Between Genotype and Laterality Defects in Primary Ciliary Dyskinesia
Morphology, Behavior, and the Sonic Hedgehog Pathway in Mouse Models of Down Syndrome
Cardiovascular Diseases Genetic Testing Program Information
POSITIVE RESULT Pathogenic Variant Identified
Aagab S00002 Aars S00003 Aars2 S00004 Aass S02483
Genome-Wide Association Study for Acute Otitis Media in Children Identifies FNDC1 As Disease Contributing Gene
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
EXAMPLE, NEGATIVE Patient Report
Top View
Glycoproteomic Characterization of Bladder Cancer Chemoresistant Cells
The Classical Genetic and Genomic Approach to the Pathogenesis of Primary Ciliary Dyskinesia Geremek, Maciej
Emerging Genotype-Phenotype Relationships in Primary Ciliary Dyskinesia
Deleterious Genetic Variants in Ciliopathy Genes Increase Risk Of
Primary Ciliary Dyskinesia
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Nuclear Roles for Cilia-Associated Proteins
Primary Ciliary Dyskinesia: Mechanisms and Management
0901219106SI.Pdf
Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease
Zebrafish Motile Cilia As a Model for Primary Ciliary Dyskinesia
Immunochip SNP Array Identifies Novel Genetic Variants
Newborndxtm Advanced Sequencing Evaluation Disorders List
Intraflagellar Transport in Caenorhabditis Elegans: Identification of Novel Proteins and Behavioural Functions
Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia
WES Gene Package Ciliopathy.Xlsx
Cone Rod Dystrophy Precision Panel Overview Indications Clinical Utility
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In